Journal of the American Chemical Society p. 1786 - 1791 (1991)
Update date:2022-09-26
Topics:
McCullough, Kevin J.
Nakamura, Norinaga
Fujisaka, Tomohiro
Nojima, Masatomo
Kusubayasbi, Shigekazu
The ozonolyses of (E)- and (Z)-o-(2-phenyl-3-methoxy-2-propenyl)benzophenone (6), which should proceed through a common carbonyl oxide intermediate 15, afforded distinctly different reaction product mixtures, suggesting that the substrate stereochemistry
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(1934)
